Linked Data
dbSNP Id:
rs1040061177
gnomAD v2:
1-160851467-T-A
gnomAD v3:
1-160881677-T-A
gnomAD v4:
1-160881677-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160881677T>A , CM000663.2:g.160881677T>A | GRCh38 |
| NC_000001.10:g.160851467T>A , CM000663.1:g.160851467T>A | GRCh37 |
| NC_000001.9:g.159118091T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326245.4:c.405+280A>T MANE Select | ENSP00000323587.3:n.405+280A>T | |
| ENST00000326245.3:c.405+280A>T | ENSP00000323587.3:n.405+280A>T | |
| ENST00000464077.1:n.339+280A>T | ||
| NM_017625.2:c.405+280A>T | NP_060095.2:n.405+280A>T | |
| NM_017625.3:c.405+280A>T MANE Select | NP_060095.2:n.405+280A>T |